EP2272349A2 - Synergistische herbizide Zusammensetzungen - Google Patents

Synergistische herbizide Zusammensetzungen Download PDF

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Publication number
EP2272349A2
EP2272349A2 EP10183875A EP10183875A EP2272349A2 EP 2272349 A2 EP2272349 A2 EP 2272349A2 EP 10183875 A EP10183875 A EP 10183875A EP 10183875 A EP10183875 A EP 10183875A EP 2272349 A2 EP2272349 A2 EP 2272349A2
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Prior art keywords
amides
esters
well
derivatives
compatible salts
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EP10183875A
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English (en)
French (fr)
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EP2272349B1 (de
EP2272349A3 (de
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Bernd Sievernich
Horst Dieter Brix
Tim Malefyt
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BASF Agrochemical Products BV
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BASF SE
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Priority to SI200531723T priority Critical patent/SI2272349T1/sl
Priority to PL10183875T priority patent/PL2272349T3/pl
Publication of EP2272349A2 publication Critical patent/EP2272349A2/de
Publication of EP2272349A3 publication Critical patent/EP2272349A3/de
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Priority to CY20131100622T priority patent/CY1114387T1/el
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Classifications

    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
    • A01N37/22—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
    • A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
    • A01N43/10—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with sulfur as the ring hetero atom
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles

Definitions

  • the present invention relates to a synergistic herbicidal mixture comprising
  • the invention furthermore relates to herbicidal compositions comprising a herbicidally active amount of a synergistic herbicidal mixture as defined above and at least one liquid and/or solid carrier and, if desired, at least one further additive.
  • the invention relates to a method of controlling undesirable vegetation by using above defined synergistic herbicidal mixture.
  • the activity and/or the selectivity of herbicides depends on a large number of factors e.g. type of the herbicide, amount of the herbicide, formulation of the herbicide, the type of weed, the combination of crop and weed, climate, soil, etc.
  • herbicides have an effect against a broad spectrum of weeds, however do not fight a certain type of other weeds, which is also present in the crop cultures to be protected.
  • This desire may be satisfied by combination of different herbicides having a different activity profile versus undesired weeds.
  • WO 00/08938 A1 (now EP 1 104 241 B1 , Bayer CropScience) describes the use of herbicide combinations for fighting weeds in herbicide resistant oilseed rape. Certain herbicidal compositions as such are also described. Respective herbicides are to be selected from four different groups and are to be combined with herbicides to be selected from five other groups.
  • the gist of WO 00/08938 A1 is the combination of glyphosate or glufosinate with other co herbicides.
  • crops e.g. oilseed rape, canola (brassica napus)
  • the mixtures according to the invention show a synergistic effect; the compatibility of the herbicidally active compounds of components A), B) and, if desired C) for certain crop plants is generally retained.
  • component A The compounds which are embraced by component A) are the following.
  • Herbicidal imidazolinones are known e.g. from C.D.S. Tomlin, "The Pesticide Manual", 13th Edition, BCPC (2003), Index 5, 1337-1344 and https://www.hclrss.demon.co.uk/index_cn_frame.html .
  • Imidazolinones shall mean herein the compounds as mentioned above, as well as their a) salts, e.g. salts of alkaline or earth alkaline metals or ammonium or organoammonium salts, for instance, sodium, potassium, ammonium, isopropyl ammonium etc.; b) respective isomers, e.g. stereo isomers such as the respective enantiomers, in particular the respective R-or S-enantiomers (including salts, ester, amides), c) respective esters, e.g.
  • carboxylic acid C1-C8-(branched or non-branched) alkyl esters such as methylesters, ethylesters, iso propyl esters
  • respective amides e.g. carboxylic acid amides or carboxylic acid C1-C8-(branched or non-branched) mono or di alkyl amides, such as dimethylamides, diethylamides, di isopropyl amides or e) any other derivative which contains the above imidazolinone structures as structural moiety.
  • Imidazolinones are the R-isomers, e.g. R-imazamethabenz-methyl, R-imazamox , R-imazapic, R-imazapyr, R-imazaquin, R-imazethapyr, in particular R-imazamox.
  • R-isomers e.g. R-imazamethabenz-methyl, R-imazamox , R-imazapic, R-imazapyr, R-imazaquin, R-imazethapyr, in particular R-imazamox.
  • Sulfonylureas examples include nicosulfuron, tritosulfuron, mesosulfuron, cyclosulfamuron, rimsulfuron, foramsulfuron.
  • Sulfonylureas shall mean herein the compounds as mentioned above, as well as their a) salts, e.g. salts of alkaline or earth alkaline metals or ammonium or organoammonium salts, for instance, sodium, potassium, ammonium, isopropyl ammonium etc.; b) respective isomers, e.g. stereo isomers such as the respective enantiomers, c) respective esters, e.g. C1-C8-(branched or non-branched) alkyl esters, such as methylesters, ethylesters, iso propyl esters, d) respective amides, e.g. amides or C1-C8-(branched or non-branched) mono or di alkyl amides, such as dimethylamides, diethylamides, di isopropyl amides.
  • salts e.g. salts of alkaline or earth alkaline metals or am
  • Very suitable Sulfonylureas are cross spectrum sulfonylureas for example nicosulfuron, mesosulfuron, rimsulfuron or foramsulfuron.
  • sulfonamides also known as “triazolopyrimidines” or “sulfonanilide herbicides” are known from C.D.S. Tomlin, “The Pesticide Manual”, 13th Edition, BCPC (2003), Index 5, 1337-1344 , WO 02/36596 A (Dow Agrosciences LLC) and https://www.hclrss.demon.co.uk/index_cn_frame.html
  • Sulfonamides shall mean herein the compounds as mentioned above as well as their a) salts, e.g. salts of alkaline or earth alkaline metals or ammonium or organoammonium salts, for instance, sodium, potassium, ammonium, isopropyl ammonium etc.; b) their respective isomers, e.g. stereo isomers such as the respective enantiomers, c) respective esters, e.g. C1-C8-(branched or non-branched) alkyl esters, such as methylesters, ethylesters, iso propyl esters, d) respective amides, e.g. amides or C1-C8-(branched or non-branched) mono or di alkyl amides, such as dimethylamides, diethylamides, di isopropyl amides.
  • salts e.g. salts of alkaline or earth alkaline metals or ammonium or
  • Very suitable Sulfonamides are florasulam, flumetsulam, metosulam, penoxulam, cloransulam-methyl, diclosulam and N-(5,7-dimethoxy[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)-2-methoxy-4-(trifluoromethyl)- 3-pyridinesulfonamide (the latter disclosed in Research Disclosure July 2002, 1230-1231 and WO 02/36596 A (Dow Agrosciences LLC)), in particular florasulam, penoxulam and N-(5,7-dimethoxy[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)-2-methoxy-4-(trifluoromethyl)-3-pyridinesulfonamide.
  • component B The compounds which are embraced by component B) are the following.
  • Chloro acetamides, oxyacetamides and tetrazolinones as described in C.D.S. Tomlin, "The Pesticide Manual", 13th Edition, BCPC (2003), Index 5, 1337-1344 and https://www.hcirss.demon.co.uk/index_cn_frame.html .
  • Chloro Acetamides shall mean herein the compounds as such as well as a) their salts, e.g. salts of alkaline or earth alkaline metals or ammonium or organoammonium salts, for instance, sodium, potassium, ammonium, isopropyl ammonium etc. or b) their respective isomers, e.g. stereo isomers such as the respective enantiomers.
  • Suitable Chloro Acetamides are metazachlor, metolachlor, "S-metolachlor", acetochlor, dimethachlor, alachlor and dimethenamid and dimethenamid-P and pethoxamid.
  • Metazachlor herein shall mean 2-Chloro-(2',6'-dimethyl-N-pyrazol-1-yl-methyl)-acetamid in all of his crystal modifications, in particular the monoclinic Metazachlor which is described in EP 0 411 408 A (BASF Aktiengesellschaft).
  • Metolachlor herein shall mean the racemic mixture of the compound CAS RN [51218-45-2] and the compound S-metolachlor and any mixture of S-isomer of metolachlor (CAS RN [87392-12-9]) and R-isomer of metolachlor (CAS RN [178961-20-1].
  • Dimethenamid herein shall mean the compounds listed in C.D.S. Tomlin, "The Pesticide Manual", 13th Edition, BCPC (2003), Index 5, 1337-1344 and https://www.hclrss.demon.co.uk/index_cn_frame.html , in particular the S-isomer (dimethenamid-P).
  • Metazachlor Metolachlor, Acetochlor and Dimetenamid shall include herein the compounds as mentioned above as well as their salts, e.g. salts of alkaline or earth alkaline metals or ammonium or organoammonium salts, for instance, sodium, potassium, magnesium, ammonium, isopropyl ammonium etc.
  • Preferred component B) comprises Metazachlor, in particular monoclinic Metazachlor, Dimethenamid, Dimethenamid-P, Metolachlor and Quinmerac.
  • a very preferred component B) is Metazachlor, in particular monoclinic Metazachlor.
  • Further components C) may be selected from the group consisting of clomazone, atrazine (see C.D.S. Tomlin, "The Pesticide Manual", 13th Edition, BCPC (2003), Index 5, 1337-1344 and https://www.hcirss.demon.co.uk/index_cn_frame.html ) and the following compounds which usually function as "safeners”, dichlormid, benoxacor, LAB-145138, MG-191, MON-13900, cyometrinil, oxabetrinil, fluxofenim, flurazole, naphtalicacidanhydride, fenchlorim, fenchlorazol, cloquintocet (including its esters and hydrate(s)), as described in "Herbizide [Herbicides]", Hock, Fedtke, Schmidt, 1st edition, Thieme 1995 (s.
  • Preferred other components C) are clomazone, atrazin and the safeners cloquintocet (including its esters and hydrate(s)).
  • Preferred herbicidal mixtures or combinations according to the invention are the following:
  • herbicidal mixtures are the following:
  • the present invention also extends to herbicidal compositions which comprise a herbicidally active amount of a synergistic herbicidal mixture (comprising components A), B) and, if desired, C) as described above), at least one liquid and/or solid carrier and, if desired, at least one further additive, for example a surfactant, adjuvant or others.
  • a synergistic herbicidal mixture comprising components A), B) and, if desired, C) as described above
  • at least one liquid and/or solid carrier and, if desired, at least one further additive, for example a surfactant, adjuvant or others.
  • the herbicidal compositions and synergistic herbicidal mixtures according to the invention can effect very good control of broad-leaved weeds and grass weeds in many crops for example maize, cereals (for example wheat), brassica napus (canola, oilseed rape), sunflower, legumes, sugar cane, and soya without damaging the crop plants, an effect observed especially even at low rates of application.
  • cereals for example wheat
  • brassica napus canola, oilseed rape
  • sunflower legumes
  • sugar cane and soya
  • the herbicidal compositions and synergistic herbicidal mixtures according to the invention can additionally be employed in a further number of crop plants for eliminating undesirable plants.
  • the herbicidal compositions and synergistic herbicidal mixtures according to the invention can preferably be used in crops which tolerate and/or are resistant to the action of ALS herbicides, preferably those ALS herbicides according to the invention.
  • the resistance and or tolerance to said herbicides may be achieved by conventional breeding and/or by genetic engineering methods.
  • Crops which are tolerant to herbicides are known for example from EP 0 154 204 A (MGI Pharma Inc.). Such crops are for example marketed by BASF under the trade name CLEARFIELD. Examples for such crops are maize, brassica napus (canola, oilseed rape), sunflower, rice, lentils and wheat.
  • Most preferable herbicide tolerant or herbicide resistant crops according to the invention is oilseed rape, canola (brassica napus).
  • the herbicidal mixtures or compositions according to the invention for example the mixtures containing Imidazolinones as sole component A), preferably the mixtures of Imidazolinones and Chloro Acetamides, very preferably mixtures or compositions comprising Imazamox and Metazachlor or Imazamox and at least one other herbicide of the groups B) and/or C) (for example those as disclosed under M1, M1-1, M1-2, M2, M2-1, M3, M3-1, M4, M4-1, M5 and M5-1, M6, M7 and M8) and in particular mixtures of Imazamox and Chloro Acetamides (for example those as disclosed under M1, M1-1, M1-2, M2, M2-1, M3, M3-1, M4, M4-1, M5 and M5-1 are very suitable for fighting or controlling a broad spectrum of grasses and broadleaf weeds which are accompanying in general the abovementioned crops, e.g. in particular brassica napus (oil
  • the weeds in ALS-herbicide resistant or tolerant brassica napus are fighted by the herbicidal mixtures or compositions according to the invention - for example the mixtures containing Imidazolinones as sole component A), preferably the mixtures of Imidazolinones and Chloro Acetamides, very preferably mixtures of Imazamox and Chloro Acetamides (for example those as disclosed under M1, M1-1, M1-2, M2, M2-1, M3, M3-1, M4, M4-1, M5, M5-1 above) and in particular those mixtures or compositions comprising Imazamox and Metazachlor.
  • Those weeds include but are not limited to the following plant species:
  • Very suitable ALS resistant or tolerant crop / to be controlled weed / herbicide mixture (composition) combinations are the following.
  • Controlled weeds include but are not limited to the listed plant species.
  • ALS tolerant crop Herbicide Mixture Weed (Latin name) Canola Imazamox+Metazachlor Agropyron repens Geranium pussilum Sinapis alba Sisymbrium officinale Canola Imazamox+Metazachlor Agropyron repens +quinmerac Galium aparine Geranium pussilum Sinapis alba Sisymbrium officinale Canola Imazamox+Metazachlor Agropyron repens +clomazone Galium aparine Geranium pussilum Sinapis alba Sisymbrium officinale Corn, sunflower Imazamox+(Dimethenamid or Echinochloa spec.
  • Dimethenamid-p Setaria spec. Digitaria spec. Corn Imazamox+(Dimethenamid or Echinochloa spec. Dimethenamid-p)+atrazin Setaria spec. Digitaria spec. Chenopodium spec. Polygonum spec. Corn, sunflower Imazamox+(Metolachlor or Echinochloa spec. S-Metolachlor) Setaria spec. Digitaria spec. Chenopodium spec. Polygonum spec. Corn Imazamox+(Metolachlor or Echinochloa spec. S-Metolachlor)+atrazin Setaria spec. Digitaria spec. Chenopodium spec.
  • the mixtures according to the invention, or the herbicidal compositions comprising them, can be employed, for example, in the form of directly sprayable aqueous solutions, powders, suspensions, also highly-concentrated aqueous, oily or other suspensions or dispersions, emulsions, oil dispersions, pastes, dusts, materials for spreading or granules, by means of spraying, atomizing, dusting, spreading or pouring.
  • Suitable inert additives are mineral oil fractions of medium to high boiling point such as kerosene and diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, e.g. paraffins, tetrahydronaphthalene, alkylated naphthalenes and their derivatives, alkylated benzenes and their derivatives, alcohols such as methanol, ethanol, propanol, butanol and cyclohexanol, ketones such as cyclohexanone, strongly polar solvents, such as N-methylpyrrolidone and water.
  • mineral oil fractions of medium to high boiling point such as kerosene and diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, e.g. paraffins, tetrahydronaphthalene, alkylated naphthalenes and their derivatives
  • Aqueous use forms can be prepared from emulsion concentrates, suspensions, pastes, wettable powders or water-dispersible granules by adding water.
  • the substances as such or dissolved in an oil or solvent, can be homogenized in water by means of wetting agent, tackifier, dispersant or emulsifier.
  • Suitable surfactants are the alkali metal, alkaline earth metal and ammonium salts of aromatic sulfonic acids, e.g. ligno-, phenol-, naphthalene- and dibutylnaphthalenesulfonic acid, and of fatty acids, of alkyl- and alkylaryl sulfonates, of alkyl sulfates, lauryl ether sulfates and fatty alcohol sulfates, and salts of sulfated hexa-, hepta- and octadecanols, and of fatty alcohol glycol ether, condensates of sulfonated naphthalene and its derivatives with formaldehyde, condensates of naphthalene, or of the naphthalenesulfonic acids, with phenol and formaldehyde, polyoxyethylene octylphenyl ether, ethoxylated isoo
  • Powders, materials for spreading and dusts can be prepared by mixing or concomitantly grinding the synergistic herbicidal mixture or the individual active ingredients with a solid carrier.
  • Granules e.g. coated granules, impregnated granules and homogeneous granules, can be prepared by binding the active ingredients to solid carriers.
  • Solid carriers are mineral earths such as silicas, silica gels, silicates, talc, kaolin, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic material, fertilizers such as ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas and products of vegetable origin such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powders or other solid carriers.
  • concentrations of the mixtures according to the invention in the ready-to-use products can be varied within wide ranges.
  • the formulations comprise from 0.01 to 95% by weight, preferably 0.5 to 90% by weight, of the mixture according to the invention.
  • the components A) and B) and, if desired, C) can be formulated jointly, but also separately, and/or applied to the plants, their environment and/or seeds jointly or separately. It is preferable to apply the active ingredients simultaneously. However, it is also possible to apply them separately.
  • herbicidal compositions and synergistic herbicidal mixtures according to the invention may be advantageous to apply the herbicidal compositions and synergistic herbicidal mixtures according to the invention, jointly or separately, with additional other crop protection agents, for example with pesticides or agents for controlling phytopathogenic fungi or bacteria.
  • additional other crop protection agents for example with pesticides or agents for controlling phytopathogenic fungi or bacteria.
  • miscibility with mineral salt solutions which are employed for treating nutritional and trace element deficiencies.
  • Non-phytotoxic oils and oil concentrates can also be added.
  • the mixtures according to the invention and the herbicidal compositions can be applied pre- or post-emergence. It is advantageous to apply the mixtures according to the invention post emergent when the crop has in general 1 to 6 leaves.
  • application techniques may be used in which the herbicidal compositions are sprayed, with the aid of the spray apparatus, in such a way that they come into as little contact, if any, with the leaves of the sensitive crop plants while reaching the leaves of undesirable plants which grow underneath, or the bare soil (post-directed, lay-by).
  • the herbicidal mixtures or compositions according to the invention are preferably applied by foliar application.
  • Application may be effected, for example, by usual spraying techniques with water as the carrier, using amounts of spray mixture of approx.15 to 1000 l/ha.
  • the mixtures or compositions may also be applied by the so-called “low-volume” and “ultra-low-volume” methods, or in the form of so-called granules.
  • the synergistic herbicidal mixtures comprise components A), B) and, if desired, C) in such weight ratios that the synergistic effect takes place.
  • the ratios of component A) and B) in the mixture in general range from 1:0.001 to 1:500, preferably from 1:0.01 to 1:100, particularly preferably from 1:0.1 to 1:50.
  • the ratios of components A) and C) in the mixture in general range from 1:0.002 to 1:800, preferably from 1:0.003 to 1:160, particularly preferably from 1:0.02 to 1:160.
  • the rate of application of pure synergistic herbicidal mixture amounts in general to 0.1 to 5000 g/ha, preferably 1 to 3000 g/ha, in particular 5 to 2500 g/ha, of active substance (a.s.), depending on the intended aim, the season, the target plants and growth stage.
  • the cumulated rate (sum of the amounts of all active ingredients of the respective group A)) of application of the component(s) A) is usually 5 to 75 g/ha of active substance (a.s.).
  • the rate of application of the Imidazolinones is usually 0.1 to 200 g/ha, as a rule 1 to 150 g/ha, preferably 5 to 100 g/ha, of active substance (a.s.).
  • the rate of application of Imazamox is usually 0.1 to 200 g/ha, as a rule, 1 to 100 g/ha, preferably 2 to 100 g/ha, of active substance (a.s.).
  • the rate of application of the Sulfonylureas or Sulfonamides is usually 0.1 to 200 g/ha, as a rule 1 to 100 g/ha, preferably 2 to 100 g/ha, of active substance (a.s.).
  • the rate of application of component B) is usually 0.1 to 5000 g/ha, as a rule 1 to 4000 g/ha, preferably 5 to 3000 g/ha, of active substance (a.s.).
  • Chloro Acetamide - e.g. Metazachlor, Metolachlor, Dimethenamid -
  • rate of application of Chloro Acetamide - e.g. Metazachlor, Metolachlor, Dimethenamid - is usually 50 to 5000 g/ha, as a rule 75 to 3000 g/ha, preferably 100 to 2000 g/ha, of active substance (a.s.).
  • Active ingredient C Rate of application (g/ha) Dichlormid 100-600 Benoxacor 10-200 LAB 145138 50-500 MG-191 200-1000 MON-13900 (Furilazole) 10-300 Naphtalicacidanhydride 300-1000 Fenchlorim 20-500 Fenchlorazol 5-100 Mefenpyr-diethyl 5-100 Isoxadifen-ethyl 1-100 Cloquintocet-mexyl 1-50 AD 67 50-500 R 29148 50-500
  • the herbicidal compositions and synergistic herbicidal mixtures according to the invention are very useful to control a broad spectrum of grass and broadleaf weeds. This usually leads to cleaner fields and higher purity of the harvested commodity as well as to higher yields of the respective crop, in particular brassica napus (oilseed rape, canola).
  • brassica napus oilseed rape, canola seeds coming from fields treated with the herbicidal compositions and synergistic herbicidal mixtures according to the invention usually have higher seed purity. Based on current knowledge this may be due to the removal of unwanted brassica species.
  • a further advantage of the instant invention is the general reduction of tillage in the respective fields which - based on current knowledge - usually leads to less loss of soil by e.g. wind.
  • the mixtures according to the invention were applied pre- or post-emergence (foliar treatment).
  • the herbicidal compounds of component A), B) and, if desired, of component C) were applied in the formulation in which they are present as commercially available product, e.g. Beyond or PULSAR 40 which is a Trademark of BASF and which is a liquid formulation containing imazamox as active ingredient; Raptor which is a trademark of BASF and which is imazamox formulated as 70 % WG or as liquid formulation; Butisan S which is a trademark of BASF and which is 500 g/I metazachlor formulated as SC; Outlook which is a dimethenamid P containing formulation.
  • the herbicidally active compounds of components A), B) were applied in succession or jointly, in the latter case in some cases as a tank mix and in some cases as a readymix, in the form of emulsions, aqueous solutions or suspensions, the vehicle being water (200 - 400 l/ha).
  • application was effected with the aid of a mobile plot sprayer.
  • test period is specified in the respective tables.
  • the value E at which only an additive effect of the individual active ingredients is to be expected was calculated by the method of S. R. Colby (Calculating synergistic and antagonistic responses of herbicide combinations, Weeds 15, 20 pp (1967)).
  • the herbicidal mixtures according to the invention exert a greater herbicidal action than would have been expected according to Colby on the basis of the observed effects of the individual components when used alone.
  • a.i. active ingredient e.g. imazamox
  • GS Growth Stage (according to "Compendium of Growth Stage Identification Keys for Mono- and Dicotyledonous Plants - Extended BBCH scale, 2 nd Edition 1997 (ISBN 3-9520749-3-4) eval. evaluation after specified days after treatment DAT days after treatment n number of trials GC Ground Cover [% of ground] n "no" y "yes" digits underneath of product name means rate of a.i. applied [g of pure ai/ha].

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  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
EP10183875.3A 2004-04-01 2005-03-30 Synergistische herbizide Zusammensetzungen Active EP2272349B1 (de)

Priority Applications (3)

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SI200531723T SI2272349T1 (sl) 2004-04-01 2005-03-30 Sinergijsko delujoče herbicidne mešanice
PL10183875T PL2272349T3 (pl) 2004-04-01 2005-03-30 Synergistycznie działające mieszaniny chwastobójcze
CY20131100622T CY1114387T1 (el) 2004-04-01 2013-07-23 Συνεργιστικως δραστικα ζιζανιοκτονα μειγματα

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US55813104P 2004-04-01 2004-04-01
EP05731882.6A EP1734823B2 (de) 2004-04-01 2005-03-30 Synergistische herbizidmischungen
EP08160242A EP1980149B1 (de) 2004-04-01 2005-03-30 Synergistische herbizide Zusammensetzungen

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US8080497B2 (en) * 2005-12-23 2011-12-20 Basf Se Method of controlling the aquatic weed Hydrilla verticillata
UA102391C2 (en) * 2008-03-20 2013-07-10 Басф Се Herbicidal compositions comprising pyroxasulfone
SI2296466T1 (sl) * 2008-06-18 2014-05-30 Basf Se Trikomponentni herbicidni sestavki, ki vsebujejo aminopiralid in imazamoks
UA117447C2 (uk) * 2011-05-04 2018-08-10 Байєр Інтеллектуал Проперті Гмбх Застосування гербіцидів інгібіторів als для боротьби з небажаною рослинністю на площі вирощування brassica
CN102657198B (zh) * 2012-05-08 2014-03-19 陕西上格之路生物科学有限公司 一种含苯肽胺酸的杀菌增产组合物
GB2515783B (en) * 2013-07-03 2018-07-11 Rotam Agrochem Int Co Ltd Process for preparing clomazone, a form and use of the same
EP3319440A1 (de) * 2015-07-10 2018-05-16 BASF Agro B.V. Herbizidzusammensetzung mit cinmethylin, metazachlor und imazamox
RU2020133762A (ru) * 2018-03-21 2022-04-21 Адама Аган Лтд. Использование антидотов для повышения устойчивости посевов риса к гербицидам
CN109392917A (zh) * 2018-10-25 2019-03-01 浙江中山化工集团股份有限公司 一种含甲氧咪草烟和吡草胺的除草组合物
EP3897138A1 (de) * 2018-12-18 2021-10-27 BASF Agrochemical Products B.V. Herbizidkombinationen
EP3897141A1 (de) 2018-12-18 2021-10-27 BASF Agrochemical Products B.V. Herbizidkombinationen
WO2020126583A1 (en) 2018-12-18 2020-06-25 Basf Agrochemical Products B.V. Herbicidal combinations
WO2020126578A1 (en) * 2018-12-18 2020-06-25 Basf Agrochemical Products B.V. Herbicidal combinations

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EP2272350A3 (de) 2011-08-31
EP1734823B2 (de) 2017-02-22
DK2272349T3 (da) 2013-07-29
AU2005230378A1 (en) 2005-10-20
PL1734823T5 (pl) 2018-05-30
HRP20120324T1 (hr) 2012-05-31
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DK1980149T3 (da) 2012-07-02
PT1734823E (pt) 2008-11-03
HUS1600051I1 (hu) 2017-01-30
EP1980149A3 (de) 2008-12-10
HRP20130239T1 (hr) 2013-04-30
PL2272350T3 (pl) 2013-07-31
EA012412B1 (ru) 2009-10-30
LTC1980149I2 (lt) 2019-03-25
EA017749B1 (ru) 2013-02-28
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CN1937918A (zh) 2007-03-28
DK2272350T3 (da) 2013-05-27
ATE549924T1 (de) 2012-04-15
ES2313322T3 (es) 2009-03-01
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HRP20130474T1 (en) 2013-07-31
EA200900769A1 (ru) 2009-10-30
LTPA2017042I1 (lt) 2018-01-10
CY1108657T1 (el) 2014-04-09
PT2272349E (pt) 2013-07-05
PT1980149E (pt) 2012-04-23
ES2413629T3 (es) 2013-07-17
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CA2558776A1 (en) 2005-10-20
PL1980149T3 (pl) 2012-08-31
AU2005230378B2 (en) 2011-08-18
HRP20080642T3 (en) 2009-01-31
SI1980149T1 (sl) 2012-05-31
PL1734823T3 (pl) 2009-04-30
EP1734823A2 (de) 2006-12-27
EP2272349B1 (de) 2013-05-15
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EA200601817A1 (ru) 2007-04-27
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UA81727C2 (ru) 2008-01-25
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US20070281859A1 (en) 2007-12-06
SI2272349T1 (sl) 2013-07-31
EP2272350A2 (de) 2011-01-12
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